University of Kansas Medical Center · 2 months ago
Clinical Research Coordinator - Internal Medicine (Pulmonary, Critical Care and Sleep Medicine)
University of Kansas Medical Center is seeking a Clinical Research Coordinator in the Division of Pulmonary, Critical Care, and Sleep Medicine. This role is responsible for coordinating and managing clinical research studies, ensuring compliance with regulatory requirements and facilitating all aspects of study conduct including subject recruitment and data collection.
EducationHigher EducationUniversities
Responsibilities
Coordinate multiple clinical research studies, including investigator-initiated and industry-sponsored trials
Develop and maintain study-specific documents, including regulatory binders, case report forms, and data collection tools
Ensure research protocols are conducted in accordance with IRB, FDA, NIH, and institutional regulations
Monitor study progress, ensuring adherence to timelines and compliance with protocols
Identify and screen eligible participants for clinical studies based on protocol inclusion/exclusion criteria
Obtain informed consent and educate participants about study procedures, risks, and benefits
Schedule study visits, follow-ups, and coordinate necessary clinical assessments
Collect and enter accurate research data into electronic data capture (EDC) systems
Maintain compliance with Good Clinical Practice (GCP) and institutional policies
Prepare and submit regulatory documents to IRB and sponsor organizations
Assist in audits, monitoring visits, and responses to queries from regulatory agencies
Coordinate sample collection, processing, and shipping according to study requirements
Assist with study-related procedures such as pulmonary function tests, sleep studies, and vital sign monitoring under supervision
Ensure investigational products (drugs, devices) are handled per protocol and regulatory requirements
Act as a liaison between study sponsors, investigators, patients, and healthcare providers
Participate in research team meetings, sponsor calls, and professional development sessions
Provide education and training to new research personnel and clinical staff as needed
Qualification
Required
4 years of experience in health sciences, nursing, biology, or related field. Education may be substituted for experience on a year for year basis
2 years of clinical research experience
Experience with clinical research regulations (FDA, GCP, IRB, HIPAA)
Organization
Problem-solving
Communication
Computer skills
Preferred
Phlebotomy certification
4 years of clinical research experience
Experience in pulmonary, critical care, or sleep medicine research
Experience with REDCap, Epic, or similar data management systems
Benefits
Health, dental, and vision insurance
Health expense accounts with generous employer contributions
Employer-paid life insurance
Long-term disability insurance
Various additional voluntary insurance plans
Paid time off, including vacation and sick
Ten paid holidays
One paid discretionary day
Paid time off for bereavement, jury duty, military service, and parental leave
A retirement program with a generous employer contribution
Additional voluntary retirement programs (457 or 403b)
Company
University of Kansas Medical Center
The University of Kansas Medical Center strives to educate exceptional health care professionals.
H1B Sponsorship
University of Kansas Medical Center has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (72)
2024 (71)
2023 (75)
2022 (67)
2021 (67)
2020 (64)
Funding
Current Stage
Late StageTotal Funding
$27MKey Investors
Kauffman FoundationNCATS
2024-11-11Grant
2022-09-21Grant· $27M
Recent News
News-Medical.Net
2025-08-26
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